A modular tool to aggregate results from bioinformatics analyses across many samples into a single report.
/home/samson/projects/RESPONSIBILIES_TRAINING/project/nf_python_demo/nf_python_variant_splitter/R1_batch_variant_splitter_nextflow/results_demo
R1 Variant Splitter — variant summary
SNV/INDEL counts per sample (from bcftools outputs).
| Sample | snvs | indels |
|---|---|---|
| sampleA | 21 | 0 |
| sampleB | 18 | 2 |
| sampleC | 21 | 4 |